Tsai FJ - Search Results

1

Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome.

Chang CF, Li LH, Wang CH, Tsai FJ, Chen TC, Wu JY, Chen YT, Tsai AC. Chang CF, et al. Among authors: tsai fj, tsai ac. Am J Med Genet A. 2010 Sep;152A(9):2365-71. doi: 10.1002/ajmg.a.33580. Am J Med Genet A. 2010. PMID: 20803649

2

Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots.

Lai CC, Tsai CH, Tsai FJ, Wu JY, Lin WD, Lee CC. Lai CC, et al. Among authors: tsai ch, tsai fj. Clin Chem. 2002 Feb;48(2):354-6. Clin Chem. 2002. PMID: 11805018 No abstract available.

3

Rapid screening assay of congenital adrenal hyperplasia by measuring 17 alpha-hydroxyprogesterone with high-performance liquid chromatography/electrospray ionization tandem mass spectrometry from dried blood spots.

Lai CC, Tsai CH, Tsai FJ, Wu JY, Lin WD, Lee CC. Lai CC, et al. Among authors: tsai ch, tsai fj. J Clin Lab Anal. 2002;16(1):20-5. doi: 10.1002/jcla.2039. J Clin Lab Anal. 2002. PMID: 11835526 Free PMC article.

4

Lack of association of interleukin-1beta gene polymorphisms in Chinese patients with systemic lupus erythematosus.

Huang CM, Wu MC, Wu JY, Tsai FJ. Huang CM, et al. Among authors: tsai fj. Rheumatol Int. 2002 Mar;21(5):173-5. doi: 10.1007/s00296-001-0164-9. Rheumatol Int. 2002. PMID: 11958432

5

Molecular analysis of syndromic congenital heart disease using short tandem repeat markers and semiquantitative polymerase chain reaction method.

Shi YR, Hsieh KS, Wu JY, Lee CC, Tsai CH, Tsai FJ. Shi YR, et al. Among authors: tsai ch, tsai fj. Pediatr Int. 2002 Jun;44(3):264-8. doi: 10.1046/j.1442-200x.2002.01553.x. Pediatr Int. 2002. PMID: 11982893

6

Angiotensin II type 1 receptor gene adenine/cytosine1166 polymorphism is not associated with mitral valve prolapse syndrome in Taiwan Chinese.

Chou HT, Shi YR, Wu JY, Tsai FJ. Chou HT, et al. Among authors: tsai fj. Circ J. 2002 Feb;66(2):163-6. doi: 10.1253/circj.66.163. Circ J. 2002. PMID: 11999641 Free article.

7

No association of vitamin D receptor gene start codon fok 1 polymorphisms in Chinese patients with systemic lupus erythematosus.

Huang CM, Wu MC, Wu JY, Tsai FJ. Huang CM, et al. Among authors: tsai fj. J Rheumatol. 2002 Jun;29(6):1211-3. J Rheumatol. 2002. PMID: 12064837

8

Interleukin-1 receptor antagonist gene polymorphism in chinese patients with systemic lupus erythematosus.

Huang CM, Wu MC, Wu JY, Tsai FJ. Huang CM, et al. Among authors: tsai fj. Clin Rheumatol. 2002 Jun;21(3):255-7. doi: 10.1007/s10067-002-8292-5. Clin Rheumatol. 2002. PMID: 12111633

9

Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers.

Lin WD, Wu JY, Tsai FJ, Gau MT, Lee CC. Lin WD, et al. Among authors: tsai fj. J Formos Med Assoc. 2002 Aug;101(8):567-71. J Formos Med Assoc. 2002. PMID: 12440087

10

A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tarda.

Shi YR, Lee CC, Hsu YA, Wang CH, Tsai FJ. Shi YR, et al. Among authors: tsai fj. Hum Hered. 2002;54(1):54-6. doi: 10.1159/000066694. Hum Hered. 2002. PMID: 12446987

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